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F Schettini

Showing results (61-70 of 116) with videos related to

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Minerva Pediatrica|March 1, 1989
[Clinico-immunologic evaluation of a trivalent vaccine against measles, rubella and mumps]F Schettini, M M Manzionna, D De Mattia, et al.
The Pediatric Infectious Disease Journal|June 1, 1990
Age-specific prevalence of hepatitis B virus infection among children in an endemic area in southern ItalyT Stroffolini, D De Mattia, A Compagnone, et al.
Haematologica|September 8, 1999
Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemiaM Carella, G W Stewart, J F Ajetunmobi, et al.
Leukemia|February 1, 1996
Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemiasA Iolascon, M F Faienza, B Coppola, et al.
Acta Paediatrica Scandinavica|March 1, 1985
Post-natal development of protein C in full-term newbornsF Schettini, D De Mattia, M Altomare, et al.
British Journal of Haematology|November 1, 1995
High frequency of homozygous deletions of CDK4I gene in childhood acute lymphoblastic leukaemiaA Iolascon, M F Faienza, B Coppola, et al.
Minerva Pediatrica|January 1, 1996
[Oromaxillofacial changes in thalassemia major]D De Mattia, P L Pettini, V Sabato, et al.
Human Genetics|November 1, 1994
A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemiaS Filosa, W Cai, R Galanello, et al.
Scandinavian Journal of Haematology|October 1, 1986
Cytochrome b and FAD content in polymorphonuclear leucocytes in a family with X-linked chronic granulomatous diseaseS Riccardi, D Giordano, F Schettini, et al.
Angewandte Chemie (International Ed. in English)|February 14, 2013
A rare uranyl(VI)-alkyl ate complex [Li(DME)1.5]2[UO2(CH2SiMe3)4] and its comparison with a homoleptic uranium(VI)-hexaalkylLani A Seaman, Peter Hrobárik, Michael F Schettini, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
Minerva Pediatrica|March 1, 1989
[Clinico-immunologic evaluation of a trivalent vaccine against measles, rubella and mumps]F Schettini, M M Manzionna, D De Mattia, et al.
The Pediatric Infectious Disease Journal|June 1, 1990
Age-specific prevalence of hepatitis B virus infection among children in an endemic area in southern ItalyT Stroffolini, D De Mattia, A Compagnone, et al.
Haematologica|September 8, 1999
Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemiaM Carella, G W Stewart, J F Ajetunmobi, et al.
Leukemia|February 1, 1996
Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemiasA Iolascon, M F Faienza, B Coppola, et al.
Acta Paediatrica Scandinavica|March 1, 1985
Post-natal development of protein C in full-term newbornsF Schettini, D De Mattia, M Altomare, et al.
British Journal of Haematology|November 1, 1995
High frequency of homozygous deletions of CDK4I gene in childhood acute lymphoblastic leukaemiaA Iolascon, M F Faienza, B Coppola, et al.
Minerva Pediatrica|January 1, 1996
[Oromaxillofacial changes in thalassemia major]D De Mattia, P L Pettini, V Sabato, et al.
Human Genetics|November 1, 1994
A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemiaS Filosa, W Cai, R Galanello, et al.
Scandinavian Journal of Haematology|October 1, 1986
Cytochrome b and FAD content in polymorphonuclear leucocytes in a family with X-linked chronic granulomatous diseaseS Riccardi, D Giordano, F Schettini, et al.
Angewandte Chemie (International Ed. in English)|February 14, 2013
A rare uranyl(VI)-alkyl ate complex [Li(DME)1.5]2[UO2(CH2SiMe3)4] and its comparison with a homoleptic uranium(VI)-hexaalkylLani A Seaman, Peter Hrobárik, Michael F Schettini, et al.
Pageof 12